US2016816A - Manufacture of di-ammonium phosphate from solutions containing ammonium phosphate - Google Patents
Manufacture of di-ammonium phosphate from solutions containing ammonium phosphate Download PDFInfo
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- US2016816A US2016816A US578461A US57846131A US2016816A US 2016816 A US2016816 A US 2016816A US 578461 A US578461 A US 578461A US 57846131 A US57846131 A US 57846131A US 2016816 A US2016816 A US 2016816A
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- ammonium phosphate
- salt
- solution
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- ammonium
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- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 title description 37
- 239000004254 Ammonium phosphate Substances 0.000 title description 10
- 229910000148 ammonium phosphate Inorganic materials 0.000 title description 10
- 235000019289 ammonium phosphates Nutrition 0.000 title description 8
- 238000004519 manufacturing process Methods 0.000 title description 7
- 150000003839 salts Chemical class 0.000 description 42
- 239000000243 solution Substances 0.000 description 41
- LFVGISIMTYGQHF-UHFFFAOYSA-N ammonium dihydrogen phosphate Chemical compound [NH4+].OP(O)([O-])=O LFVGISIMTYGQHF-UHFFFAOYSA-N 0.000 description 29
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 28
- 229910000387 ammonium dihydrogen phosphate Inorganic materials 0.000 description 28
- 235000019837 monoammonium phosphate Nutrition 0.000 description 28
- 239000006012 monoammonium phosphate Substances 0.000 description 28
- 239000007787 solid Substances 0.000 description 26
- 238000000034 method Methods 0.000 description 20
- 238000001704 evaporation Methods 0.000 description 15
- 239000000203 mixture Substances 0.000 description 15
- 239000006200 vaporizer Substances 0.000 description 14
- 229910021529 ammonia Inorganic materials 0.000 description 13
- 238000001816 cooling Methods 0.000 description 13
- 229920006395 saturated elastomer Polymers 0.000 description 12
- 229940010556 ammonium phosphate Drugs 0.000 description 9
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 8
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 8
- 239000001166 ammonium sulphate Substances 0.000 description 8
- 235000011130 ammonium sulphate Nutrition 0.000 description 8
- 239000013078 crystal Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 229910019142 PO4 Inorganic materials 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 6
- 235000021317 phosphate Nutrition 0.000 description 6
- 239000010452 phosphate Substances 0.000 description 6
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 229910021653 sulphate ion Inorganic materials 0.000 description 5
- 238000002425 crystallisation Methods 0.000 description 4
- 230000008025 crystallization Effects 0.000 description 4
- 239000012266 salt solution Substances 0.000 description 4
- 239000012047 saturated solution Substances 0.000 description 4
- 239000005696 Diammonium phosphate Substances 0.000 description 3
- 229910000388 diammonium phosphate Inorganic materials 0.000 description 3
- 235000019838 diammonium phosphate Nutrition 0.000 description 3
- 239000011833 salt mixture Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- KNQKRMVYLDOGCT-UHFFFAOYSA-N ammonium phosphate sulfate Chemical compound [NH4+].[NH4+].OP(O)([O-])=O.OS([O-])(=O)=O KNQKRMVYLDOGCT-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- NPQXVJAQVIQXHJ-UHFFFAOYSA-N triazanium sulfuric acid phosphate Chemical compound [NH4+].[NH4+].[NH4+].OS(O)(=O)=O.[O-]P([O-])([O-])=O NPQXVJAQVIQXHJ-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000498 cooling water Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B25/00—Phosphorus; Compounds thereof
- C01B25/16—Oxyacids of phosphorus; Salts thereof
- C01B25/26—Phosphates
- C01B25/28—Ammonium phosphates
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B25/00—Phosphorus; Compounds thereof
- C01B25/16—Oxyacids of phosphorus; Salts thereof
- C01B25/26—Phosphates
- C01B25/38—Condensed phosphates
- C01B25/40—Polyphosphates
- C01B25/405—Polyphosphates of ammonium
Definitions
- One object of my invention is to provide improvements in the production of solid mono-ammonium phosphate or salt mixtures containing mono-ammonium phosphate which avoids the danger of clogging by'solidication of the salt pap from which the solid mono-ammonium phosphate ⁇ is obtained.
- My new process consists in mixing the hot saltv pap leaving the vaporizer rst of all Witha cold saturated or almost saturated mono-ammonium phosphate solution and only then separating the- 40 mother lye from the crystals contained in the salt pap.
- a further object of my present invention is to provide improvements in the production of solid di-ammonium phosphate from solutions which contain mono-ammonium phosphate which will likewise overcome the above described diiiiculty.
- This latter improved process consists essential- 1y in evaporating in a vaporizer the mono-ammonium phosphate containing solution which is to be worked to a solid salt, and then passing the salt pap withdrawn from the vaporizer without substantial cooling into an agitator which contains coldsaturated or almost saturated di-ammonium phosphate mother lye.
- the salt pap withdrawn from the vaporizer is cooleddown without forming solid lumps whereupon the separated salt which consists mainly of mono-ammonium phosphate is converted into di-ammonium phosphate by being further stirred withthe mother lye to which ammonia preferably in the gaseous form is added, the di-ammonium phosphate being then separated from the mother lye by centrifugals or the like.
- the great advantage of the process consists in the fact that as the salt pap removed from the 10 vaporizer is stirred into the cold saturated mother lye it is cooled down. At the same time the concentrated ⁇ mother lye adhering thereto is so strongly diluted that the salt pap no longer solidies on cooling down. ⁇ It is thereby possible with- 15 out diiliculty to treat the salt pap removed from the vaporizer and mixed with saturated mother lye in a centrifugal or the like for the purpose of separating the mother lye from the crystals.
- the new process described herein can also be carried 20 out by converting the salt mixture consisting mainly of mono-ammonium phosphate which is iirst formed in the evaporation stages into diammonium phosphate by stirring with saturated di-ammonium phosphate solution with addition 25 of ammonia, simultaneously with the cooling down by admixing the cold solution, which leads to a great simplification of the process.
- the salt pap diluted with thecold saturated 30 mother lye can be freed of a part of the mother lye before the treatment with the ammoniacal diammonium phosphate solution, for instance by stopping the agitator for a short time and allowing the salt to settle.
- My invention also permits 35 the above described operations that is, the dilution of the hot salt pap with cold almost saturated mother lye and the subsequent treatment with ammoniacal saturated di-ammonium phosphate solution. to be combined into a single operation 4o whereby a further simplication rof the process herein described is obtained.
- the hot salt pap leaving the vaporizer is stirred directly into a saturated or almost saturated di-ammonium phosphate solution and the mixture then 45 treated with ammonia.
- the improved process herein described may be used for working practically all solutions which contain ammonium phosphate, particularly solutions which contain ammonium sulphate and am- 50 monium phosphate as produced for instance in processes for removing ammonia and hydrogen sulphide from gases according to my co-pending patent application, Serial No. 426,771 led February 7, 1930. 55
- a further object of the invention is to provide an apparatus for carrying out the process according to the invention.
- the salt solution to be treated is passed through a pipe I to the evaporating vessel 2 of a vaporizer which is connected by a forward pipe 3 and a return pipe 4 with the heater 5 which in the ordinary manner has a series oi heating tubes 6 through which the liquid to be vaporized is passed in 'a direction from bottom to top.
- 'Ihe heater tubes 6 are swept over externally by steam which is supplied through the pipe 'I and withdrawn through the pipe 8.
- the salt solution heated in the heater 5 is returned through the pipe 4 into the evaporating vessels 2 in which a low pressure is maintained by means of an air pump not shown in the drawe ing.
- the vapours forming from the solution leave the vessel 2 through the pipe 9.
- the salt solution is conned in the vaporizer until solid crystals separate out from it. If an ammonium sulphate-ammonium phosphate solu tion is being worked from which it is desired to regain the two ammonium salts in the same proportion in which they were present in the primary solution, it is preferable to employ the process described in my patent application Serial N0. 533,807.
- the salt pap forming in the vaporizer is progressively or intermittently withdrawn through apipe II controlled by a valve I0 into a vessel I2 in which the solid crystals are separated from the main part of the mother lye withdrawn therewith which is returned back into the vaporizer.
- the still iiuid salt pap remaining in the vessel I2 is then passed into a vessel I5 by means of a pump I5 through the pipe I4 which is provided with a heat insulating jacket and is controlled by the valve I3.
- a certain quantity i1 of a cold almost saturated mother lye In this vessel there is a certain quantity i1 of a cold almost saturated mother lye.
- the salt pap is introduced into the mother lye contained in the vessel I6 whereby it is cooled. During this introduction the mixture is stirred by means of an agitator I9 driven by a motor I8.
- the cooled salt pap passes from the vessel I6 through the pipe 24 controlled by the valve 23 into a vessel 25 likewise provided with an agitator 25.
- this vessel there is a saturated ammoniacal dieammonium phosphate solution which is passed to the vessel 26 from the supply tank 2'! through a pipe 28.
- the vessel 26 serves to convert the mono-ammonium phosphate contained in the cooled salt pap wholly or partially into di-ammonium phosphate when it is desired to produce solid di-ammonium phosphate or a mixture of mono-ammonium phosphate and di-ammonium phosphate.
- ammonia gas is passed from below through the liquid in the vessel 26, through the perforated pipe 29.
- ammonium crystals dissolve in a saturated diammonium phosphate solution, whilst at the same time the di-ammonium phosphate crystals formed separate out.
- the vapours formed by the passage of ammonia through the liquid in the vessel 26 can escape through the discharge pipe 30.
- the ammonia contained in the vapours is preferably precipitated and returned again into the liquid in the vessel 26 or used again at another suitable stage in the process.
- Example 1 11.1 parts of an o C. mixture consisting oi 2.1 parts water, 5.4 parts ammonium sulphate and 3.6 parts monoammonium phosphate were stirred into 15.7 cbm. of a 20 warm ammonium sulphate mono-ammonium phosphate mother lye almost saturated at 20 C. and consisting of 11.0 parts water, 5.4 parts ammonium sulphate and 3.6 parts mono-ammonium phosphate. Thereby the temperature of the solution with the unsaturated salt contained therein rose to 40 C. After cooling down to 20 C. 6.6 parts salt of the following' composition separated out: 30.4% sulphuric acid, 49.6% phosphoric acid, 18.05% amlnonia, 2.2% water, i. e.
- the salt 'formed may be used in this form as a fertilizer but can also be converted into a mixture of ammonium sulphate and di-amrnonium phosphate according to my process.
- Example 2 In 6.0 cbm. of a di-ammonium phosphate ammonium sulphate solution of 20 C. and having a composition 17% di-ammonium phosphate, 27% sulphate and 56% water, 8.0 parts of an 80 C. mixture consisting of 3.6 parts sulphate, 2.4 parts mono-ammonium phosphate and 2.0 parts water were introduced, and then ammonia in the form of concentrated gas added during further continued stirring. The temperature rose thereby to 48 C. When the ammonia was no longer completely absorbed and the solution smelled of ammonia it Was cooled down to 20 and the separated salt fitered 011. There were Cil produced 6.0 cbm. mother lye with 2.19 parts sulphate and 0.70 part di-ammonium phosphate together with 4.7 parts solid salt with 52.7% diammonium phosphate, 45.9% ammonium sulphate and 1.4% water.
- a method of .producing solid mono-ammonium phosphate from solutions containing mono-ammonium phosphate comprising evaporating the solution containing mono-ammonium phosphate up to the crystallization point of the salt by heating the solution, separating salt pap formed from the evaporating operation While hot, mixing the Withdrawn salt pap While still hot from the evaporating operation with a cold saturated solution of mono-ammonium phosphate to cool the pap Without solidication into a solid mass and separating the solid salt from the cooling mixture.
- a process for producing solid di-ammonium phosphate from mono-ammonium phosphate containing solutions comprising evaporating the solution containing mono-ammonium phosphate up to crystallization of the salt by heating the solution, separating the crystals from the largest part of the mother lye While hot therefrom, mixing the hot salt pap produced thereby and While still hot from the evaporating operation With a cold saturated solution of mono-ammonium phosphate and thereby cooling the pap without solidiiication into a solid mass, treating the mixture With a saturated di-ammonium phosphate solution in the presence of ammonia, and separating the solid salt from the mixture.
- a process for producing solid mono-ammonium phosphate from mono-ammonium phosphate containing solutions comprising evaporating the solution containing mono-ammonium phosphate up to crystallization of the salt by heating the solution, separating the crystals from the largest part of the mother lye While still hot, mixing the hot salt papproduced thereby and While still hot from the evaporating operation with a cold saturated solution of mono-ammonium phosphate and thereby cooling the pap Without solidification into a solid mass, cooling the mixture and separating the solid salt from the cooling mixture.
- a process for producing solid cli-ammonium phosphate from solutions containing mainly mono-ammonium phosphate comprising evaporating by heating a solution of mono-ammonium phosphate up to crystallization of the salt, separating salt pap formed from the evaporating solution While hot, mixing the hot salt pap produced thereby and While still hot from the evaporating operation with a cold saturated solution of monoammonium phosphate and thereby cooling the pap Without solidication thereof into a solid mass, cooling the mixture, and treating the mixture with a saturated cli-ammonium phosphate solution in the presence of ammonia and separating the solid salt from the solution.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Fertilizers (AREA)
Description
@et 8, i935., c. J. HANSEN 2 Mw MANUFACTURE OF DI-AMMONIUM PHOSPHATE FROM SOLUTIODS CONTAINING AMMONIUM PHOSPHATE Filed Dec. 2, 1951 fffr/ Patented Oct. 8, 1935 UNITED ASTATES PATENT OFFICE i MANUFACTURE OF DI-AMMONIUM PHOS- PHATE FROM SOLUTIONS CONTAINING AMMONIUM PHOSPHATE Application December 2, 1931, Serial No. 578,461 In Germany'December 3, 1930 4 Claims. (Cl. 23--107) This invention relates to the manufacture of solid ammonium phosphate from solutions containing ammonium phosphate and more particularly to the production of solid di-ammonium 5 phosphate from solutions containing this compound.
In my co-pending patent application Serial No. 533,807 led May 7th 1931 I have described a process for obtaining solid di-ammonium phosphate 10 from ammonium phosphate solutions which consists in evaporating the ammonium phosphate containing salt solution in a vaporizer, removing from the vaporizer the salt mixture formed thereby and treating with an ammoniacal saturated diammonium phosphate solution for the purpose of converting the mono-ammonium phosphate into di-ammonium phosphate. In technically carying out this process certain diiliculties have arisen in so far as in practice it is not always possible to separate the mother lye with simple means from the salt pap removed from the vaporizer. In practice the mother lye cannot be prevented from cooling down somewhat after being removed from the vaporiz'er. In this way such considerable quantities of solid salt separate from the mother lye that in certain cases the whole mass stiffens to a solid lump, thereby clogging the centrifugals and the pipe systems.
One object of my invention is to provide improvements in the production of solid mono-ammonium phosphate or salt mixtures containing mono-ammonium phosphate which avoids the danger of clogging by'solidication of the salt pap from which the solid mono-ammonium phosphate` is obtained.
My new process consists in mixing the hot saltv pap leaving the vaporizer rst of all Witha cold saturated or almost saturated mono-ammonium phosphate solution and only then separating the- 40 mother lye from the crystals contained in the salt pap.
A further object of my present invention is to provide improvements in the production of solid di-ammonium phosphate from solutions which contain mono-ammonium phosphate which will likewise overcome the above described diiiiculty.
This latter improved process consists essential- 1y in evaporating in a vaporizer the mono-ammonium phosphate containing solution which is to be worked to a solid salt, and then passing the salt pap withdrawn from the vaporizer without substantial cooling into an agitator which contains coldsaturated or almost saturated di-ammonium phosphate mother lye. In this case also l the salt pap withdrawn from the vaporizer is cooleddown without forming solid lumps whereupon the separated salt which consists mainly of mono-ammonium phosphate is converted into di-ammonium phosphate by being further stirred withthe mother lye to which ammonia preferably in the gaseous form is added, the di-ammonium phosphate being then separated from the mother lye by centrifugals or the like.
The great advantage of the process consists in the fact that as the salt pap removed from the 10 vaporizer is stirred into the cold saturated mother lye it is cooled down. At the same time the concentrated `mother lye adhering thereto is so strongly diluted that the salt pap no longer solidies on cooling down.` It is thereby possible with- 15 out diiliculty to treat the salt pap removed from the vaporizer and mixed with saturated mother lye in a centrifugal or the like for the purpose of separating the mother lye from the crystals. The new process described herein can also be carried 20 out by converting the salt mixture consisting mainly of mono-ammonium phosphate which is iirst formed in the evaporation stages into diammonium phosphate by stirring with saturated di-ammonium phosphate solution with addition 25 of ammonia, simultaneously with the cooling down by admixing the cold solution, which leads to a great simplification of the process.
With particular advantage according to the inl vention the salt pap diluted with thecold saturated 30 mother lye can be freed of a part of the mother lye before the treatment with the ammoniacal diammonium phosphate solution, for instance by stopping the agitator for a short time and allowing the salt to settle. My invention also permits 35 the above described operations that is, the dilution of the hot salt pap with cold almost saturated mother lye and the subsequent treatment with ammoniacal saturated di-ammonium phosphate solution. to be combined into a single operation 4o whereby a further simplication rof the process herein described is obtained. For this purpose the hot salt pap leaving the vaporizer is stirred directly into a saturated or almost saturated di-ammonium phosphate solution and the mixture then 45 treated with ammonia.
The improved process herein described may be used for working practically all solutions which contain ammonium phosphate, particularly solutions which contain ammonium sulphate and am- 50 monium phosphate as produced for instance in processes for removing ammonia and hydrogen sulphide from gases according to my co-pending patent application, Serial No. 426,771 led February 7, 1930. 55
A further object of the invention is to provide an apparatus for carrying out the process according to the invention.
With these and other objects of the invention in view I will now describe the nature of the present invention on the lines of the accompanying drawing which shows a side elevation and partial longitudinal section through an apparatus Y suitable for carrying out the process according to the invention.
In the apparatus shown in the drawing the salt solution to be treated is passed through a pipe I to the evaporating vessel 2 of a vaporizer which is connected by a forward pipe 3 and a return pipe 4 with the heater 5 which in the ordinary manner has a series oi heating tubes 6 through which the liquid to be vaporized is passed in 'a direction from bottom to top. 'Ihe heater tubes 6 are swept over externally by steam which is supplied through the pipe 'I and withdrawn through the pipe 8.
The salt solution heated in the heater 5 is returned through the pipe 4 into the evaporating vessels 2 in which a low pressure is maintained by means of an air pump not shown in the drawe ing. The vapours forming from the solution leave the vessel 2 through the pipe 9.
The salt solution is conned in the vaporizer until solid crystals separate out from it. If an ammonium sulphate-ammonium phosphate solu tion is being worked from which it is desired to regain the two ammonium salts in the same proportion in which they were present in the primary solution, it is preferable to employ the process described in my patent application Serial N0. 533,807.
The salt pap forming in the vaporizer is progressively or intermittently withdrawn through apipe II controlled by a valve I0 into a vessel I2 in which the solid crystals are separated from the main part of the mother lye withdrawn therewith which is returned back into the vaporizer. The still iiuid salt pap remaining in the vessel I2 is then passed into a vessel I5 by means of a pump I5 through the pipe I4 which is provided with a heat insulating jacket and is controlled by the valve I3. In this vessel there is a certain quantity i1 of a cold almost saturated mother lye. The salt pap is introduced into the mother lye contained in the vessel I6 whereby it is cooled. During this introduction the mixture is stirred by means of an agitator I9 driven by a motor I8.
Cold saturated mother lye ilows into the Vessel I 6 through the pipe 20. For cooling the liquid in the Vessel I6 the latter is also provided with pipe coils 2l through whose outer connection pipes 22, steam or cooling water maybe passed as desired.
II di-ammonium phosphate is to be obtained as a final product the cooled salt pap passes from the vessel I6 through the pipe 24 controlled by the valve 23 into a vessel 25 likewise provided with an agitator 25. In this vessel there is a saturated ammoniacal dieammonium phosphate solution which is passed to the vessel 26 from the supply tank 2'! through a pipe 28.
The vessel 26 serves to convert the mono-ammonium phosphate contained in the cooled salt pap wholly or partially into di-ammonium phosphate when it is desired to produce solid di-ammonium phosphate or a mixture of mono-ammonium phosphate and di-ammonium phosphate. For this purpose ammonia gas is passed from below through the liquid in the vessel 26, through the perforated pipe 29. In the vessel 26 the mono,-
ammonium crystals dissolve in a saturated diammonium phosphate solution, whilst at the same time the di-ammonium phosphate crystals formed separate out.
The vapours formed by the passage of ammonia through the liquid in the vessel 26 can escape through the discharge pipe 30. The ammonia contained in the vapours is preferably precipitated and returned again into the liquid in the vessel 26 or used again at another suitable stage in the process.
As soon as the conversion of the mono-ammonirun phosphate into di-ammonium phosphate in the vessel 26 has reached the desired amount the liquid contained in the vessel 26 is passed through the pipe 32 controlled by a valve 3| into a centrifugal 33 in which the salts are separated from the mother lye. Themanner in which the process according to the invention is carried out may be illustrated by two following examples:
Example 1 11.1 parts of an o C. mixture consisting oi 2.1 parts water, 5.4 parts ammonium sulphate and 3.6 parts monoammonium phosphate were stirred into 15.7 cbm. of a 20 warm ammonium sulphate mono-ammonium phosphate mother lye almost saturated at 20 C. and consisting of 11.0 parts water, 5.4 parts ammonium sulphate and 3.6 parts mono-ammonium phosphate. Thereby the temperature of the solution with the unsaturated salt contained therein rose to 40 C. After cooling down to 20 C. 6.6 parts salt of the following' composition separated out: 30.4% sulphuric acid, 49.6% phosphoric acid, 18.05% amlnonia, 2.2% water, i. e. about 41% ammonium sulphate and 57.5% mono-ammonium phosphate. 18.2 cbm. were yielded as a mother lye containing 6.1 parts ammonium-,sulphate and 1.5 parts mono-ammonium phosphate.
The salt 'formed may be used in this form as a fertilizer but can also be converted into a mixture of ammonium sulphate and di-amrnonium phosphate according to my process.
For this purpose 5.0 parts of the above obtained salt were introduced into 5.0 cbm. of a 20 C. warm solution of 17%l di-ammonium phosphate, 27% ammonium sulphate and 56% water, after which concentrated gaseous ammonia was introduced during continued stirring until the solution smelled of ammonia. The temperature rose thereby to 55 C. After the conversion had taken place the solution was iiltered. There were produced 5.4 cbm. of an ammonium sulphate di-ammonium phosphate mother lye saturated at 20% with about 1.2 parts di-ammonimn phosphate and 3.0 parts ammonium sulphate and 4.3 parts salt consisting of 19.2% sulphate, 75.0% di-ammonium phosphate and 5.8% water.
Example 2 In 6.0 cbm. of a di-ammonium phosphate ammonium sulphate solution of 20 C. and having a composition 17% di-ammonium phosphate, 27% sulphate and 56% water, 8.0 parts of an 80 C. mixture consisting of 3.6 parts sulphate, 2.4 parts mono-ammonium phosphate and 2.0 parts water were introduced, and then ammonia in the form of concentrated gas added during further continued stirring. The temperature rose thereby to 48 C. When the ammonia was no longer completely absorbed and the solution smelled of ammonia it Was cooled down to 20 and the separated salt fitered 011. There were Cil produced 6.0 cbm. mother lye with 2.19 parts sulphate and 0.70 part di-ammonium phosphate together with 4.7 parts solid salt with 52.7% diammonium phosphate, 45.9% ammonium sulphate and 1.4% water.
The invention as herein above set forth is embodied in a particular form but may be Variously embodied Within the scope of the claims hereinafter made.
I claim:
1. A method of .producing solid mono-ammonium phosphate from solutions containing mono-ammonium phosphate comprising evaporating the solution containing mono-ammonium phosphate up to the crystallization point of the salt by heating the solution, separating salt pap formed from the evaporating operation While hot, mixing the Withdrawn salt pap While still hot from the evaporating operation with a cold saturated solution of mono-ammonium phosphate to cool the pap Without solidication into a solid mass and separating the solid salt from the cooling mixture.
2. A process for producing solid di-ammonium phosphate from mono-ammonium phosphate containing solutions comprising evaporating the solution containing mono-ammonium phosphate up to crystallization of the salt by heating the solution, separating the crystals from the largest part of the mother lye While hot therefrom, mixing the hot salt pap produced thereby and While still hot from the evaporating operation With a cold saturated solution of mono-ammonium phosphate and thereby cooling the pap without solidiiication into a solid mass, treating the mixture With a saturated di-ammonium phosphate solution in the presence of ammonia, and separating the solid salt from the mixture.
3. A process for producing solid mono-ammonium phosphate from mono-ammonium phosphate containing solutions comprising evaporating the solution containing mono-ammonium phosphate up to crystallization of the salt by heating the solution, separating the crystals from the largest part of the mother lye While still hot, mixing the hot salt papproduced thereby and While still hot from the evaporating operation with a cold saturated solution of mono-ammonium phosphate and thereby cooling the pap Without solidification into a solid mass, cooling the mixture and separating the solid salt from the cooling mixture.
4. A process for producing solid cli-ammonium phosphate from solutions containing mainly mono-ammonium phosphate, comprising evaporating by heating a solution of mono-ammonium phosphate up to crystallization of the salt, separating salt pap formed from the evaporating solution While hot, mixing the hot salt pap produced thereby and While still hot from the evaporating operation with a cold saturated solution of monoammonium phosphate and thereby cooling the pap Without solidication thereof into a solid mass, cooling the mixture, and treating the mixture with a saturated cli-ammonium phosphate solution in the presence of ammonia and separating the solid salt from the solution.
CHRISTIAN JOHANNES HANSEN.
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2946655A (en) * | 1957-08-22 | 1960-07-26 | Koppers Co Inc | Production of diammonium phosphate |
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1931
- 1931-12-02 US US578461A patent/US2016816A/en not_active Expired - Lifetime
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2946655A (en) * | 1957-08-22 | 1960-07-26 | Koppers Co Inc | Production of diammonium phosphate |
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